Canonical Allele Identifier: CA354610408

Gene: TF

Linked Data

• MyVariant Identifiers: chr3:g.133494376G>C (hg19) ; chr3:g.133775532G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.133775532G>C , CM000665.2:g.133775532G>C	GRCh38
NC_000003.11:g.133494376G>C , CM000665.1:g.133494376G>C	GRCh37
NC_000003.10:g.134977066G>C	NCBI36
NG_013080.1:g.34400G>C
NG_013080.2:g.118535G>C

Transcript Alleles

HGVS	Amino-acid change
ENST00000402696.9:c.1787G>C MANE Select	ENSP00000385834.3:p.Cys596Ser
ENST00000402696.7:c.1787G>C	ENSP00000385834.3:p.Cys596Ser
ENST00000461695.1:c.518G>C
ENST00000467842.1:n.2781G>C
NM_001063.3:c.1787G>C	NP_001054.1:p.Cys596Ser
XM_011513100.1:c.1787G>C	XP_011511402.1:p.Cys596Ser
NM_001354703.1:c.1655G>C	NP_001341632.1:p.Cys552Ser
NM_001354704.1:c.1406G>C	NP_001341633.1:p.Cys469Ser
NM_001063.4:c.1787G>C MANE Select	NP_001054.2:p.Cys596Ser
NM_001354703.2:c.1655G>C	NP_001341632.2:p.Cys552Ser
NM_001354704.2:c.1406G>C	NP_001341633.2:p.Cys469Ser